Y-mAbs to Host Virtual Radiopharmaceutical R&D Update on May 28, 2025

Rhea-AI Summary

Y-mAbs Therapeutics (NASDAQ: YMAB) has announced a virtual Radiopharmaceutical R&D update scheduled for May 28, 2025, at 8:00 a.m. ET. The 90-minute presentation will cover several key areas including:

• Part A clinical data from the ongoing Phase 1 GD2-SADA clinical trial (Trial 1001), featuring pharmacokinetic and dosimetry data
• Updates on nonclinical optimization studies for the GD2-SADA asset and clinical implementation plans
• The company's Radiopharmaceutical pipeline strategy, including new planned target programs and timelines

The event will be accessible via webcast on Y-mAbs' Investor Relations website and will remain archived for at least 30 days.

PRINCETON, N.J., May 13, 2025 (GLOBE NEWSWIRE) -- Y-mAbs Therapeutics, Inc. (the “Company” or “Y-mAbs”) (Nasdaq: YMAB), a commercial-stage biopharmaceutical company focused on the development and commercialization of novel radioimmunotherapy and antibody-based therapeutic products for the treatment of cancer, today announced it will hold a virtual Radiopharmaceutical R&D update at 8:00 a.m. ET on Wednesday, May 28, 2025.

During the virtual Radiopharmaceutical R&D update, Y-mAbs will discuss: Part A clinical data from the Company’s ongoing Phase 1 GD2-SADA clinical trial (Trial 1001), including pharmacokinetic and dosimetry data; updates around the Company's nonclinical optimization studies for the GD2-SADA asset and plans for clinical implementation; and the Company’s Radiopharmaceutical pipeline strategy, including new planned target programs and anticipated timelines.

The duration of the virtual Radiopharmaceutical R&D update is expected to be 90 minutes. A live audio webcast of the call will be available on the Investor Relations section of the Company’s website at https://ir.ymabs.com/events-and-presentations/events. The webcast will be archived for at least 30 days.

About Y-mAbs
Y-mAbs is a commercial-stage biopharmaceutical company focused on the development and commercialization of novel, radioimmunotherapy and antibody-based therapeutic cancer products. The Company’s technologies include its investigational Self-Assembly DisAssembly (“SADA”) Pretargeted Radioimmunotherapy Platform (“PRIT”) and bispecific antibodies generated using the Y-BiClone platform. The Company’s broad and advanced product pipeline includes the anti-GD2 therapy DANYELZA® (naxitamab-gqgk), the first FDA-approved treatment for patients with relapsed or refractory high-risk neuroblastoma in the bone or bone marrow after a partial response, minor response, or stable disease to prior therapy.

Forward-Looking Statements
Statements in this press release about future expectations, plans and prospects, as well as any other statements regarding matters that are not historical facts, may constitute “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Such statements include, but are not limited to, statements about our business model, including financial outlook for 2025 and beyond. Words such as ‘‘anticipate,’’ ‘‘believe,’’ “contemplate,” ‘‘continue,’’ ‘‘could,’’ ‘‘estimate,’’ ‘‘expect,’’ “hope,” ‘‘intend,’’ ‘‘may,’’ ‘‘might,’’ ‘‘plan,’’ ‘‘potential,’’ ‘‘predict,’’ ‘‘project,’’ ‘‘should,’’ ‘‘target,’’ “will,” ‘‘would’,’ “guidance,” “goal,” “objective,” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. The Company’s business is subject to risks and uncertainties affecting the Company including those described in the “Risk Factors” section included in the Company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2024, and the Company’s Quarterly Report on Form 10-Q for the quarterly periods ended March 31, 2025, and future filings and reports by the Company. Any forward-looking statements contained in this press release speak only as of the date hereof, and the Company undertakes no obligation to update any forward-looking statement, whether as a result of new information, future events or otherwise.

SADA^®, SADA PRIT™, DANYELZA^® and Y-mAbs^® are registered trademarks of Y-mAbs Therapeutics, Inc.

Investor Contact:
Courtney Dugan
VP, Head of Investor Relations
cdu@ymabs.com

FAQ

When is Y-mAbs (YMAB) hosting its Radiopharmaceutical R&D update in 2025?

Y-mAbs is hosting its virtual Radiopharmaceutical R&D update on Wednesday, May 28, 2025, at 8:00 a.m. ET.

What topics will be covered in Y-mAbs' (YMAB) May 2025 R&D update?

The update will cover Phase 1 GD2-SADA clinical trial data, nonclinical optimization studies updates, and the company's Radiopharmaceutical pipeline strategy including new target programs and timelines.

How long will Y-mAbs' (YMAB) May 2025 Radiopharmaceutical R&D presentation last?

The virtual Radiopharmaceutical R&D update is expected to last 90 minutes.

Where can investors access Y-mAbs' (YMAB) May 2025 R&D presentation?

The presentation will be accessible via webcast on Y-mAbs' Investor Relations website at https://ir.ymabs.com/events-and-presentations/events and will be archived for at least 30 days.